ClinVar Miner

Submissions for variant NM_001303.4(COX10):c.*151_*152del

dbSNP: rs200239586
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000332249 SCV000400631 benign Mitochondrial complex IV deficiency, nuclear type 1 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000386652 SCV000400632 benign Leigh syndrome 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001541165 SCV001759127 benign not provided 2019-09-02 criteria provided, single submitter clinical testing

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